Title:
Method of treating nitrate-induced tolerance
Document Type and Number:
United States Patent 6225315

Abstract:
The present invention relates to methods for treating nitrate-induced tolerance in a mammal by administering a nitrate-induced tolerance treating amount of a compound of formulae (I), (II), (III) (IV), (V), (VI), (VII), (VIII), (IX), (XA) or (XB) as defined herein, or the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites or stereoisomers thereof. The invention also relates to pharmaceutical compositions for the treatment of nitrate-induced tolerance in a mammal comprising a nitrate-induced tolerance treating amount of a compound of formulae (I), (II), (III) (IV), (V), (VI), (VII), (VIII), (IX), (XA) or (XB) as defined herein, or the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites or stereoisomers thereof, and a pharmaceutically acceptable vehicle, diluent or carrier. The invention further relates to methods of preventing nitrate-induced tolerance in a mammal comprising administering a nitrate-induced tolerance preventing amount of a cGMP PDE inhibitor.
Inventors:
Ellis, Peter (Sandwich, GB)
Application Number:
09/442821
Publication Date:
05/01/2001
Filing Date:
11/18/1999
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Assignee:
Pfizer INC (New York, NY)
Primary Class:
International Classes:
A61K31/495; A61K31/496; A61K31/4985; A61K31/505; A61K31/517; A61K31/519; A61K31/495; A61K31/505
Field of Search:
514/258, 514/259, 514/250
US Patent References:
5250534Pyrazolopyrimidinone antianginal agentsOctober, 1993Bell et al.514/258
5272147Pyrazolopyrimidinone antianginal agentsDecember, 1993Bell et al.514/234.2
52946126-heterocyclyl pyrazolo [3,4-d]pyrimidin-4-ones and compositions and method of use thereofMarch, 1994Bacon et al.514/234.2
5346901Pyrazolopyrimidinone antianginal agentsSeptember, 1994Bell et al.514/258
5482941Quinazolinone antianginal agentsJanuary, 1996Terrett514/253
5488055Substituted N-cycloalkylmethyl-1H-pyrazolo(3,4-b)quinolin-4 amines and compositions and methods of use thereofJanuary, 1996Kumar et al.514/293
55411876-heterocycyclyl pyrazolo[3,4-d]pyrimidin-4-ones and compositions and method of use thereofJuly, 1996Bacon et al.514/258
5591742Pyridopyrimidinone antianginal agentsJanuary, 1997Bell et al.514/234.5
5614530Substituted N-arylmethyl and heterocyclmethyl-1H-pyrazolo[3,4-b]quinolin-4-amines and compositions and methods of use thereofMarch, 1997Kumar et al.514/293
56566296-substituted pyrazolo (3,4-d)pyrimidin-4-ones and compositions and methods of use thereofAugust, 1997Bacon et al.514/234.5
5734053Purinone antianginal agentsMarch, 1998Terrett544/277
57365486-aryl pyrazolo 3,4-D! pyrimidin-4-ones and compositions and method of use thereofApril, 1998Bacon et al.514/258
Foreign References:
WO/1993/012095June, 1939QUINAZOLINONE ANTIANGINAL AGENTS
WO/1993/007149April, 1993PYRAZOLOPYRIMIDINONE ANTIANGINAL AGENTS
WO/1993/006104April, 1993PYRAZOLOPYRIMIDINONE ANTIANGINAL AGENTS
WO/1994/000453January, 1994PURINONE ANTIANGINAL AGENTS
WO/1994/028902December, 1994PYRAZOLOPYRIMIDINONES FOR THE TREATMENT OF IMPOTENCE
WO/1996/028429September, 19966-SUBSTITUTED PYRAZOLO PYRIMIDIN-4-ONES AND COMPOSITIONS AND METHODS OF USE THEREOF
WO/1996/028446September, 1996SUBSTITUTED N-CYCLOALKYLMETHYL-1H-PYRAZOLOQUINOLIN-4 AMINES AND COMPOSITIONS AND METHODS OF USE THEREOF
WO/1996/028448September, 19966-ARYL PYRAZOLOPYRIMIDIN-4-ONES AND COMPOSITIONS AND METHODS OF USE THEREOF
WO/1998/049166November, 1998PYRAZOLOPYRIMIDINONES WHICH INHIBIT TYPE 5 CYCLIC GUANOSINE 3',5'-MONOPHOSPHATE PHOSPHODIESTERASE (cGMP PDE5) FOR THE TREATMENT OF SEXUAL DYSFUNCTION
Other References:
Anderson, T. L. G. et al. Journal of Cardiovascular Pharmacology, vol. 18 (2): pp. 237-242 (1991).
De Garavilla, L., et al. Journal of Molecular and Cellular Cardiology, vol. 24 (Suppl. 3): S37 (1992).
De Garavilla, L. et al. European Journal of Pharmacology, vol. 313 (1-2): pp. 89-96 (1996).
Merkel, L. A. et al. European Journal of Pharmacology, vol. 216 (1): pp. 29-35 (1992).
Pagani, E. D. et al. European Journal of Pharmacology, vol. 243 (2): pp. 141-147 (1993).
Saeki, T. et al. Journal of Pharmacology and Experimental Therapeutics, vol. 272 (2): pp. 825-831 (1995).
Silver, P. J. et al. European Journal of Pharmacology, vol. 199 (1): pp. 141-142 (1991).
Szilvassy, Z. et al. Journal of Molecular and Cellular Cardiology, vol. 28 (5): A97 (1996).
Thompson, W. J. et al. Biochem. 10:311 (1971).
Thompson, W. J. et al. Biochem. 18:5228 (1979).
Primary Examiner:
Henley III, Raymond
Attorney, Agent or Firm:
Richardson, Peter C.
Benson, Gregg C.
Eispert, Jennifer A.
Parent Case Data:
CROSSREFERENCE TO RELATED APPLICATION

This application claims priority from U.S. Provisional Patent Application No. 60/110,335 filed Nov. 30, 1998, the benefit of which is hereby claimed under 37 C.F.R. §1.78(a)(3).

Claims:
What is claimed is:

1. A method of treating nitrate-induced tolerance in a mammal comprising administering to said mammal a nitrate-induced tolerance treating amount of

a compound of formula (I) ##STR13##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R1 is H, C1 -C3 alkyl, C3 -C5 cycloalkyl or C1 -C3 perfluoroalkyl;

R2 is H, C1 -C6 alkyl optionally substituted by OH, C1 -C3 alkoxy or C3 -C6 cycloalkyl, or C1 -C3 perfluoroalkyl;

R3 is C1 -C6 alkyl, C3 -C6 alkenyl, C3 -C6 alkynyl, C3 -C7 cycloalkyl, C1 -C6 perfluoroalkyl or (C3 -C6 cycloalkyl)C1 -C6 alkyl;

R4 taken together with the nitrogen atom to which it is attached completes a 4-N--(R6)-piperazinyl group;

R5 is H, C1 -C4 alkyl, C1 -C3 alkoxy, NR7 R8 or CONR7 R8 ;

R6 is H, C1 -C6 alkyl, (C1 -C3 alkoxy)C2 -C6 alkyl, hydroxy C2 -C6 alkyl, (R7 R8 N)C2 -C6 alkyl, (R7 R8 NCO)C1 -C6 alkyl, CONR7 R8, CSNR7 R8 or C(NH)NR7 R8 ; and

R7 and R8 are each independently H, C1 -C4 alkyl, (C1 -C3 alkoxy)C2 -C4 alkyl or hydroxy C2 -C4 alkyl;

a compound of formula (II) ##STR14##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R9 is H, C1 -C3 alkyl optionally substituted with one or more fluoro substituents, or C3 -C5 cycloalkyl;

R10 is H or C1 -C6 alkyl optionally substituted with one or more fluoro substituents or with C3 -C6 cycloalkyl;

R11 is C1 -C6 alkyl optionally substituted with one or more fluoro substituents or with C3 -C6 cycloalkyl, or C3 -C5 cycloalkyl, or C3 -C6 alkenyl, or C3 -C6 alkynyl;

R12 is C1 -C4 alkyl optionally substituted with OH, NR13 R14, CN, CONR13 R14 or with CO2 R15, or C2 -C4 alkenyl optionally substituted with CN, CONR13 R14 or with CO2 R15, or C2 -C4 alkanoyl optionally substituted with NR13 R14, or hydroxy C2 -C4 alky optionally substituted with NR13 R14, or (C2 -C3 alkoxy)C1 -C2 alkyl optionally substituted with OH or NR13 R14, or CONR13 R14, or CO2 R15, or halo, or NR13 R14, or NHSO2 NR13 R14, or NHSO2 R16, or phenyl or heterocyclyl either of which is optionally substituted with methyl;

R13 and R14 are each independently H, C1 -C4 alkyl, or together with the nitrogen atom to which they are attached form a pyrrolidinyl, piperidino, morpholino, 4-(NR17)-piperazinyl or imidazolyl group wherein said group is optionally substituted with methyl or hydroxy;

R15 is H or C1 -C4 alkyl;

R16 is C1 -C3 alkyl optionally substituted with NR13 R14 ; and

R17 is H, C1 -C3 alkyl optionally substituted with phenyl, or hydroxy C2 -C3 alkyl, or C1 -C4 alkanoyl;

a compound of formula (III) ##STR15##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein: R1, R2, R3 and R5 are as previously described for said formula (I); R18 taken together with the nitrogen to which it is attached completes a pyrrolidinyl, piperidino or morpholino group;

a compound of formula (IV) ##STR16##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R19 is C1 -C4 alkyl;

R20 is C2 -C4 alkyl;

R21 is H or SO2 NR22 R23 ;

R22 and R23 together with the nitrogen atom to which they are attached form a pyrrolidino, piperidino, morpholino or 4-N--(R24)-1-piperazinyl group; and

R24 is H or C1 -C3 alkyl;

a compound of formula (V) ##STR17##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R25 is H, C1 -C4 alkyl, C1 -C4 alkoxy or CONR29 R30 ;

R26 is H or C1 -C4 alkyl;

R27 is C2 -C4 alkyl;

R28 is H, C2 -C4 alkanoyl optionally substituted with NR31 R32, or (hydroxy)C2 -C4 alkyl optionally substituted with NR31 R32, or CHCHCO2 R33, or CHCHCONR31 R32, or CH2 CH2 CO2 R33, or CH2 CH2 CONR31 R32, or SO2 NR31 R32, or SO2 NH(CH2)n NR31 R32 or imidazolyl;

R29 and R30 are each independently H or C1 -C4 alkyl;

R31 and R32 are each independently H or C1 -C4 alkyl, or together with the nitrogen atom to which they are attached form a pyrrolidino, piperidino, morpholino or 4-(NR34)-1-piperazinyl group wherein any of said groups is optionally substituted with CONR29 R30 ;

R33 is H or C1 -C4 alkyl;

R34 is H, C1 -C3 alkyl or (hydroxy)C2 -C3 alkyl; and

n is 2, 3 or 4; and provided that R28 is not H when R25 is H, C1 -C4 alkyl or C1 -C4 alkoxy;

a compound of formula (VI) ##STR18##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R35 is H, C1 -C4 alkyl, CN or CONR29 R30 ;

R36 is C2 -C4 alkyl;

R37 is SO2 NR38 R39, NO2, NH2, NHCOR42, NHSO2 R42 or N(SO2 R42)2 ;

R38 and R39 are each independently selected from H and C1 -C4 alkyl optionally substituted with CO2 R43, OH, pyridyl, 5-isoxazolin-3-onyl, morpholino or 1-imidazolidin-2-onyl, or together with the nitrogen atom to which they are attached form a pyrrolidino, piperidino, morpholino, 1-pyrazolyl or 4-(NR44)-1-piperazinyl group wherein any of said groups may optionally be substituted with one or two substituents selected from C1 -C4 alkyl, CO2 R43, NH2 and OH;

R42 is C1 -C4 alkyl or pyridyl;

R43 is H or C1 -C4 alkyl; and

R44 is H, C1 -C4 alkyl or (hydroxy)C2 -C3 alkyl;

a compound of formula (VII) ##STR19##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R45 is C1 -C6 alkyl;

R46 is H, methyl or ethyl;

R47 is C2 -C4 alkyl;

R48 is C1 -C4 alkyl optionally substituted with NR49 R50, CN, CONR49 R50 or CO2 R51 ; C2 -C4 alkenyl optionally substituted with CN, CONR49 R50 or CO2 R51 ; C2 -C4 alkanoyl optionally substituted with NR49 R50 ; SO2 NR49 R50 ; CONR49 R50 ; CO2 R51 ; or halo;

R49 and R50 are each independently H or C1 -C4 alkyl, or together with the nitrogen atom to which they are attached form a pyrrolidino, piperidino, morpholino, 4-(NR52)-1-piperazinyl or 1-imidazolyl group wherein said group is optionally substituted by one or two C1 -C4 alkyl groups;

R51 is H or C1 -C4 alkyl; and

R52 is H, C1 -C3 alkyl or hydroxy C2 -C3 alkyl;

a compound of formula (VIII) ##STR20##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R53 is methyl or ethyl;

R54 is ethyl or n-propyl;

R55 and R56 are each independently H or C1 -C6 alkyl optionally substituted with C5 -C7 cycloalkyl or with morpholino; or

a compound of formula (IX) ##STR21##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R57 is hydrogen, halogen or C1-6 alkyl;

R58 is hydrogen, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, halo C1-6 alkyl, C3-8 cycloalkyl, C3-8 cycloalkyl C1-3 alkyl, aryl C1-3 alkyl or heteroaryl C1-3 alkyl;

R59 is an optionally substituted monocyclic aromatic ring selected from benzene, thiophene, furan and pyridine or an optionally substituted bicyclic ring ##STR22##

attached to the rest of the molecule via one of the benzene ring carbon atoms and wherein the fused ring A is a 5- or 6-membered ring which may be saturated or partially or fully unsaturated and comprises carbon atoms and optionally one or two heteroatoms selected from oxygen, sulphur and nitrogen; and

R60 is hydrogen or C1-3 alkyl, or R58 and R60 together represent a 3- or 4-membered alkyl or alkenyl chain; or

a compound of formulae (XA) or (XB) ##STR23##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R61 is C1 -C3 alkyl substituted with C3 -C6 cycloalkyl, CONR65 R66 or a N-linked heterocyclic group selected from pyrazolyl, imidazolyl, triazolyl, pyrrolidinyl, piperidinyl, morpholinyl and 4-R67 -piperazinyl; (CH2)p Het or (CH2)q Ar;

R62 is C1 -C6 alkyl;

R63 is C1 -C6 alkyl optionally substituted with C1 -C4 alkoxy;

R64 is SO2 NR68 R69 ;

R65 and R66 are each independently selected from H and C1 -C4 alkyl optionally substituted with C1 -C4 alkoxy, or, together with the nitrogen atom to which they are attached, form a pyrrolidinyl, piperidinyl, morpholinyl or 4-R67 -piperazinyl group;

R68 and R69, together with the nitrogen atom to which they are attached, form a 4-R70 -piperazinyl group;

R67 is C1 -C4 alkyl;

R70 is H or C1 -C4 alkyl optionally substituted with OH, C1 -C4 alkoxy or CONH2 ;

Het is a C-linked 6-membered heterocyclic group containing one or two nitrogen atoms, optionally in the form of of its mono-N-oxide, or a C-linked 5-membered heterocyclic group containing from one to four heteroatoms selected from nitrogen, oxygen and sulfur, wherein either of said heterocyclic groups is optionally substituted with one or two substituents selected from C1 -C4 alkyl optionally substituted with C1 -C4 alkoxy, C1 -C4 alkoxy, halo and NH2 ;

Ar is phenyl optionally substituted with one or two substituents selected from C1 -C4 alkyl, C1 -C4 alkoxy, halo, CN, CONH2, NO2, NH2, NHSO2 (C1 -C4 alkyl) and SO2 NH2 ; and

p and q are each independently 0 or 1.



2. A method as defined in claim 1 wherein in said formula (I) R1 is H, methyl or ethyl; R2 is C1 -C3 alkyl optionally substituted by OH or methoxy; R3 is C2 -C3 alkyl or allyl; R4 taken together with the nitrogen atom to which it is attached completes a piperidino or 4-N--(R6)-piperazinyl group; R5 is H, NR7 R8 or CONR7 R8 ; R6 is H, C1 -C3 alkyl, hydroxy C2 -C3 alkyl, CONR7 R8, CSNR7 R8 or C(NH)NR7 R8 ; and R7 and R8 are each independently H or methyl.

3. A method as defined in claim 2 wherein R1 is methyl; R2 is n-propyl; R3 is ethyl, n-propyl or allyl; R4 taken together with the nitrogen atom to which it is attached forms a 4-N--(R6)-piperazinyl group; R5 is H; and R6 is H, C1 -C3 alkyl or 2-hydroxyethyl.

4. A method as defined in claim 2 wherein R1 is methyl; R2 is n-propyl; R3 is ethyl; R5 is H; and R6 is methyl.

5. A method as defined in claim 1 wherein in said formula (II) R9 is H, methyl or ethyl; R10 is C1 -C3 alkyl; R11 is C2 -C3 alkyl; R12 is C1 -C2 alkyl optionally substituted with OH, NR13 R14, CONR13 R14 or with CO2 R15, acetyl optionally substituted with NR13 R14, or hydroxy ethyl substituted with NR13 R14, or ethoxymethyl optionally substituted with OH or with NR13 R14, or CHCHCN, or CHCHCONR13 R14, or CHCHCO2 R15, or CO2 H, or Br, or NR13 R14, or CONR13 R14, or NHSO2 NR13 R14, or NHSO2 R16, or pyridinyl or imidazolyl either of which is optionally substituted with methyl; R13 and R14 are each independently H, methyl or ethyl, or together with the nitrogen atom to which they are attached form a piperidino, morpholino, 4-(NR17)-1-piperazinyl or imidazolyl group wherein said group is optionally substituted with methyl or hydroxy; R15 is H or t-butyl; R16 is methyl or CH2 CH2 CH2 NR13 R14 ; and R17 is H, methyl, benzyl, 2-hydroxyethyl or acetyl.

6. A method as defined in claim 5 wherein R9 is methyl; R10 is n-propyl; R11 is ethyl or n-propyl; R12 is CH2 NR13 R14, CH2 OCH2 CH2 NR13 R14, CH2 OCH2 CH3, CH2 OCH2 CH2 OH, COCH2 NR13 R14, CH(OH)CH2 NR13 R14, CHCHCON(CH3)2, CHCHCO2 R15, CO2 H, CONR13 R14, NHSO2 NR13 R14, NHSO2 CH2 CH2 CH2 NR13 R14, 2-pyridyl, 1-imidazolyl or 1-methyl-2-imidazolyl; and R13 and R14 together with the nitrogen atom to which they are attached form a piperidino, 4-hydroxypiperidino, morpholino, 4-(NR17)-1-piperazinyl or 2-methyl-1-imidazolyl group.

7. A method as defined in claim 1 wherein in said formula (III) R1 is H, methyl or ethyl; R2 is C1 -C3 alkyl optionally substituted by OH or methoxy; R3 is C2 -C3 alkyl or allyl; R18 taken together with the nitrogen atom to which it is attached completes a piperidino group; R5 is H, NR7 R8 or CONR7 R8 ; and R7 and R8 are each independently H or methyl.

8. A method as defined in claim 1 wherein in said formula (IV) R19 and R20 are each independently ethyl or n-propyl; and R22 and R23 together with the nitrogen atom to which they are attached form a 4-N--(R24)-1-piperazinyl group.

9. A method as defined in claim 8 wherein R19 is n-propyl; R20 is ethyl; and R21 is 1-piperazinylsulphonyl or 4-methyl-1-piperazinylsulfonyl.

10. A method as defined in claim 1 wherein in said formula (V) R25 is H, methoxy or CONR29 R30 ; R26 is H or methyl; R27 is ethyl or n-propyl; R28 is H, acetyl optionally substituted with NR31 R32, or hydroxyethyl substituted with NR31 R32, or CHCHCO2 R33, or CHCHCONR31 R32, or CH2 CH2 CO2 R33, or SO2 NR31 R32, or SO2 NH(CH2)3 NR31 R32 or 1-imidazolyl; R29 and R30 are each independently H or ethyl; R31 and R32 together with the nitrogen atom to which they are attached form a piperidino, 4-carbamoylpiperidino, morpholino or 4-(NR34)-1-piperazinyl group; R33 is H or t-butyl; and R34 is H, methyl or 2-hydroxyethyl; provided that R28 is not H when R25 is H or methoxy.

11. A method as defined in claim 10 wherein R25 is methyl, CONH2 or CONHCH2 CH3 ; R26 is H; R28 is H, acetyl, 1-hydroxy-2-(NR31 R32)ethyl, CHCHCO2 C(CH3)3, or CHCHCONR31 R32, or SO2 NR31 R32 or 1-midazolyl; R31 and R32 together with the nitrogen atom to which they are attached form a 4-(NR34)-1-piperazinyl group; and R34 is methyl or 2-hydroxyethyl; provided that R28 is not H when R25 is methyl.

12. A method as defined in claim 1 wherein in said formula (VI) R35 is H, n-propyl, CN or CONH2 ; R36 is ethyl; R37 is SO2 NR40 R41, NO2, NH2, NHCOCH(CH3)2, NHSO2 CH(CH3)2, NHSO2 (3-pyridyl) or N[SO2 (3-pyridyl)]2 ; R40 is H, methyl or 2-hydroxyethyl; R41 is methyl optionally substituted with 2-pyridyl or 5-isoxazolin-3-onyl, or ethyl 2-substituted with OH, CO2 CH2 CH3, morpholino or with 1-imidazolidin-2-onyl; or R40 and R41 together with the nitrogen atom to which they are attached form a (4-CO2 R43)piperidino, 5-amino-3-hydroxy-1-pyrazolyl or 4-(NR44)-1-piperazinyl group; R43 is H or ethyl; and R44 is H, methyl or 2-hydroxyethyl.

13. A method as defined in claim 12 wherein R35 is n-propyl or CN; R37 is SO2 NR40 R41, NHSO2 CH(CH3)2, NHSO2 (3-pyridyl) or N[SO2 (3-pyridyl)]2 ; and R40 is H or methyl and R41 is methyl, ethyl 2-substituted with CO2 CH2 CH3, morpholino or 1-imidazolidin-2-onyl, or R40 and R41 together with the nitrogen atom to which they are attached form a (4-CO2 R43)piperidino or 4-(NR44)-1-piperazinyl group.

14. A method as defined in claim 1 wherein in said formula (VII) R45 is n-propyl; R46 is H or methyl; R47 is ethyl or n-propyl; R48 is ethyl substituted with CONR49 R50 or CO2 R51, vinyl substituted with CONR49 R50 or CO2 R51, acetyl substituted with NR49 R50, or SO2 NR49 R50, or CONR49 R50, or CO2 R51, or bromo; R49 and R50 together with the nitrogen atom to which they are attached form a morpholino, 4-(NR52)-1-piperazinyl or 2,4-dimethyl-1-imidazolyl group; R51 is H or t-butyl; and R52 is methyl or 2-hydroxyethyl.

15. A method as defined in claim 1 wherein in said formula (VIII) R55 is H, methyl or ethyl; and R56 is C1 -C6 alkyl optionally substituted with cyclohexyl or with morpholino.

16. A method as defined in claim 1 wherein in said formula (IX) R57 is H, halogen or C1 -C6 alkyl.

17. A method as defined in claim 16 wherein R57 is H.

18. A method as claimed in claim 16 wherein R57 is halogen.

19. A method as defined in claim 18 wherein R57 is fluorine.

20. A method as defined in claim 1 wherein in said formula (IX) R58 is hydrogen, C1-6 alkyl, halo C1-6 alkyl, C3-8 cycloalkyl, C3-8 cycloalkyl C1-3 alkyl, aryl C1-3 alkyl or heteroaryl C1-3 alkyl.

21. A method as defined in claim 1 wherein in said formula (IX) R58 is hydrogen, C1-4 alkyl, halo C1-4 alkyl, C3-6 cycloalkyl, C3-6 cycloalkylmethyl, pyridyl C1-3 alkyl, furyl C1-3 alkyl or optionally substituted benzyl.

22. A method as defined in claim 1 wherein in said formula (IX) R58 is C1-4 alkyl, C3-6 cycloalkyl, or C3-6 cycloalkylmethyl.

23. A method as defined in claim 21 wherein R58 is fluorobenzyl.

24. A method as defined in claim 1 wherein in said formula (IX) R59 is an optionally substituted benzene, thiophene, furan, pyridine or naphthalene ring or an optionally substituted bicyclic ring ##STR24##

where m is 1 or 2 and X and Y are each CH2 or O.



25. A method as defined in claim 1 wherein in said formula (IX) R59 is a benzene ring substituted by C1-3 alkoxy, or by C1-3 alkoxy and halogen.

26. A method as defined in claim 1 wherein in said formula (IX) R59 is 3,4-methylenedioxyphenyl.

27. A method as defined in claim 1 wherein in said formula (IX) R60 is hydrogen.

28. A method as defined in claim 1 wherein in said formula (IX) R58 and R60 together are a 3-membered alkyl chain.

29. A method as defined in claim 1 wherein in said formulae (XA) and (XB) R61 is C1 -C2 alkyl substituted with C3 -C5 cycloalkyl, CONR65 R66 or a N-linked heterocyclic group selected from pyrazolyl, triazolyl, morpholinyl and 4-R67 -piperazinyl; (CH2)p Het or (CH2)q Ar; R65 is H; R66 is C1 -C4 alkyl optionally substituted with C1 -C4 alkoxy, or, R65 and R66 together with the nitrogen atom to which they are attached, form a morpholinyl group; Het is selected from pyridinyl, 1-oxidopyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, imidazolyl, isoxazolyl, thiazolyl, triazolyl and oxadiazolyl, any of which is optionally substituted with one or two substituents selected from CH3, CH2 CH2 OCH3, OCH3 and NH2.

30. A method as defined in claim 29 wherein in said formulae (XA) and (XB) R61 is C1 -C2 alkyl substituted with cyclobutyl, CONR65 R66, pyrazol-1-yl, 1,2,3-triazol-1-yl, 1,2,4-triazol-1-yl, morpholin-4-yl or 4-methylpiperazin-1-yl; pyrimidin-2-yl; CH2 Het or (CH2)q Ar; R62 is C1 -C3 alkyl; R63 is C1 -C3 alkyl optionally substituted with C1 -C2 alkoxy; R65 is H; R66 is C1 -C2 alkyl optionally substituted with C1 -C2 alkoxy, or R65 and R66 together with the nitrogen atom to which they are attached, form a morpholin-4-yl group; R70 is C1 -C2 alkyl optionally monosubstituted with OH, OCH3 or CONH2 ; Het is selected from pyridin-2-yl, 1-oxidopyridin-2-yl, pyridin-3-yl, pyridazin-3-yl, pyridazin-4-yl, pyrimidin-4-yl, pyrimidin-5-yl, pyrazin-2-yl, 3-methoxypyridin-2-yl, 6-aminopyridin-2-yl, 1-methylimidazol-2-yl, 3,5-dimethylisoxazol-4-yl, 2-methylthiazol-4-yl, 1-methyl-1,2,4-triazol-5-yl, 1-(2-methoxyethyl)-1,2,4-triazol-5-yl, 4-methyl-1,2,4-triazol-3-yl, 3-methyl-1,2,4-triazol-5-yl, 1,2,4-oxadiazol-3-yl and 5-methyl-1,2,4-oxadiazol-3-yl; Ar is selected from phenyl, 4-chlorophenyl, 4-bromophenyl, 2-cyanophenyl, 2-carbamoylphenyl, 4-carbamoylphenyl, 2-nitrophenyl, 4-nitrophenyl, 2-aminophenyl, 4-aminophenyl, 2-methanesulfonamidophenyl, 4-methanesulfonamidophenyl, 4-ethanesulfonamidophenyl, 4-(prop-2-ylsulfonamido)phenyl and 4-sulfamoylphenyl.

31. A method as defined in claim 30 wherein in said formulae (XA) and (XB) R61 is cyclobutylmethyl, morpholin-4-ylcarbonylmethyl, 2-(morpholin-4-yl)ethyl, pyrimidin-2-yl, CH2 Het or (CH2)q Ar; R62 is CH2 CH3 or CH2 CH2 CH3 ; R63 is CH2 CH3, CH2 CH2 CH3 or CH2 CH2 OCH3 ; R70 is CH3, CH2 CH3 or CH2 CH2 OH; Het is selected form pyridin-2-yl, pyridazin-3-yl, pyrazin-2-yl, 3-methoxypyridin-2-yl, 6-aminopyridin-2-yl, 1-methylimidazol-2-yl, 3,5-dimethylisoxazol-4-yl, 1-methyl-1,2,4-triazol-5-yl, 1-(2-methoxyethyl)-1,2,4-triazol-5-yl and 5-methyl-1,2,4-oxadiazol-3-yl; Ar is selected from phenyl, 2-aminophenyl, 2-methanesulfon-amidophenyl, 4-methanesulfonamidophenyl, 4-ethanesulfonamidophenyl and 4-(prop-2-ylsulfonamido)phenyl.

32. A method as defined in claim 1 wherein said compound of said formula (I) is selected from:

5-[2-allyloxy-5-(4-methylpiperazinylsulfonyl)phenyl]-1-methyl-3-n-propyl-1, 6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one,

5-[2-ethoxy-5-(piperazinylsulfonyl)phenyl]-1-methyl-3-n-propyl-1,6-dihydro- 7H-pyrazolo[4,3-d]pyrimidin-7-one,

5-[2-ethoxy-5-(4-methylpiperazinylsulfonyl)phenyl]-1-methyl-3-n-propyl-1,6- dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one,

5-{2-ethoxy-5-[4-(2-propyl)piperazinylsulfonyl]phenyl}-1-methyl-3-n-propyl- 1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one,

5-{2-ethoxy-5-[4-(2-hydroxyethyl)piperazinylsulfonyl]phenyl}-1-methyl-3-n-p ropyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one,

1-methyl-5-[5-piperazinylsulfonyl)-2-n-propoxy-phenyl]-3-n-propyl-1,6-dihyd ro-7H-pyrazolo[4,3-d]pyrimidin-7-one,

5-{5-[4-(2-hydroxyethyl)piperazinylsulfonyl]-2-n-propoxyphenyl}-1-methyl-3- n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one and the pharmaceutically acceptable salts thereof.



33. A method as defined in claim 32 wherein said compound is 5-[2-ethoxy-5-(4-methylpiperazinylsulfonyl)phenyl]-1-methyl-3-n-propyl-1,6 -dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one.

34. A method as defined in claim 33 wherein said compound is a citrate salt of 5-[2-ethoxy-5-(4-methylpiperazinylsulfonyl)phenyl]-1-methyl-3-n-propyl-1,6 -dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one.

35. A method as defined in claim 1 wherein said compound of said formula (II) is selected from:

5-[2-ethoxy-5-(1-methyl-2-imidazolyl)phenyl]-1-methyl-3-n-propyl-1,6-dihydr o-7H-pyrazolo[4,3-d]pyrimidin-7-one,

5-[2-ethoxy-5-(4-methyl-1-piperazinylcarbonyl)phenyl]-1-methyl-3-n-propyl-1 ,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one,

5-[5-(4-acetyl-1-piperazinyl)acetyl-2-ethoxyphenyl]-1-methyl-3-n-propyl-1,6 -dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one,

5-(2-ethoxy-5-morpholinoacetylphenyl]-1-methyl-3-n-propyl-1,6-dihydro-7H-py razolo[4,3-d]pyrimidin-7-one,

5-(5-morpholinoacetyl-2-propoxyphenyl)-1-methyl-3-n-propyl-1,6-dihydro-7H-p yrazolo[4,3-d]pyrimidin-7-one and the pharmaceutically acceptable salts thereof.



36. A method as defined in claim 1 wherein said compound of said formula (V) is selected from:

2-{2-ethoxy-5-[4-(2-hydroxyethyl)-1-piperazinylsulfonyl]phenyl}-8-methylqui nazolin-4(3H)-one,

2-{5-[4-(2-hydroxyethyl)-1-piperazinylsulfonyl]2-n-propoxyphenyl}-8-methylq uinazolin-4(3H)-one,

8-methyl-2-{5-[2-(4-methyl-1-piperazinylcarbonyl)ethenyl]-2-n-propoxyphenyl }quinazolin-4(3H)-one,

8-carbamoyl-2-{2-ethoxy-5-[4-(2-hydroxyethyl)-1-piperazinylsulfonyl]phenyl} quinazolin-4(3H)-one,

8-ethylcarbamoyl-2-(2-n-propoxyphenyl)quinazolin-4(3H)-one and the pharmaceutically acceptable salts thereof.



37. A method as defined in claim 1 wherein said compound of said formula (VI) is selected from:

2-[2-ethoxy-5-(4-ethoxycarbonylpiperidinosulfonyl)phenyl]-8-n-propylpyrido[ 3,2-d]pyrimidin-4(3H)-one,

2-[5-(4-carboxypiperidinosulfonyl)-2-ethoxyphenyl]-8-n-propylpyrido[3,2-d]p yrimidin-4(3H)-one,

2-{2-ethoxy-5-[4-(2-hydroxyethyl)-1-piperazinylsulfonyl]phenyl}-8-n-propylp yrido[3,2-d]pyrimidin-4(3H)-one,

2-{2-ethoxy-5-[(bis-3-pyridylsulfonyl)amino]phenyl}-8-n-propylpyrido[3,2-d] pyrimidin-4(3H)-one and the pharmaceutically acceptable salts thereof.



38. A method as defined in claim 1 wherein said compound of said formula (VII) is selected from:

6-(5-bromo-2-n-propoxyphenyl)-3-methyl-1-n-propyl-1,5-dihydro-4H-pyrazolo[3 ,4-d]pyrimidin-4-one,

3-methyl-6-(5-morpholinosulfonyl-2-n-propoxyphenyl)-1-n-propyl-1,5-dihydro- 4H-pyrazolo[3,4-d]pyrimidin-4-one,

6-[5-(2-carboxyvinyl)-2-n-propoxyphenyl]-3-methyl-1-n-propyl-1,5-dihydro-4H -pyrazolo[3,4-d]pyrimidin-4-one,

6-[5-(2-t-butoxycarbonylvinyl)-2-n-propoxyphenyl]-3-methyl-1-n-propyl-1,5-d ihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one,

3-methyl-6-[5-(2-morpholinocarbonylvinyl)-2-n-propoxyphenyl]-1-n-propyl-1,5 -dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one,

3-methyl-6-[5-(2-morpholinocarbonylethyl)-2-n-propoxyphenyl]-1-n-propyl-1,5 -dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one and the pharmaceutically acceptable salts thereof.



39. A method as defined in claim 1 wherein said compound of said formula (VIII) is selected from:

5-[2-ethoxy-5-(3-morpholinopropylsulfamoyl)-phenyl]-1,3-dimethyl-1,6-dihydr o-7H-pyrazolo[4,3-d]pyrimidin-7-one,

1-ethyl-5-[5-(n-hexylsulfamoyl)-2-n-propoxyphenyl]-3-methyl-1,6-dihydro-7H- pyrazolo[4,3-d]pyrimidin-7-one,

1-ethyl-5-(5-diethylsulfamoyl-2-n-pro-poxyphenyl)-3-methyl-1,6-dihydro-7H-p yrazolo[4,3-d]pyrimidin-7-one,

5-[5-(N-cyclohexylmethyl-N-methylsulfamoyl)-2-n-propoxyphenyl]1-ethyl-3-met hyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one and the pharmaceutically acceptable salts thereof.



40. A method as defined in claim 1 wherein said compound of said formula (IX) is selected from:

cis-2,3,6,7,12,12a-hexahydro-2-(4-pyridylmethyl)-6-(3,4-methylenedioxypheny l)-pyrazino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione,

cis-2,3,6,7,12,12a-hexahydro-6-(2,3-dihydrobenzo[b]furan-5-yl)-2-methyl-pyr azino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione,

cis-2,3,6,7,12,12a-hexahydro-6-(5-bromo-2-thienyl)-2-methyl-pyrazino[2',1': 6,1]pyrido[3,4-b]indole-1,4-dione,

cis-2,3,6,7,12,12a-hexahydro-2-butyl-6-(4-methylphenyl)pyrazino[2',1': 6,1]pyrido[3,4-b]indole-1,4-dione,

cis-2,3,6,7,12,12a-hexahydro-2-cyclopropyl-6-(3,4-methylenedioxyphenyl)-pyr azino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione,

(3S,6R,12aR)-2,3,6,7,12,12a-hexahydro-3-methyl-6-(3,4-methylenedioxyphenyl) -pyrazino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione,

(3S,6R,12aR)-2,3,6,7,12,12a-hexahydro-2,3-dimethyl-6-(3,4-methylenedioxyphe nyl)-pyrazino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione,

(6R,12aR)-2,3,6,7,12,12a-hexahydro-2-isopropyl-6-(3,4-methylenedioxyphenyl) -pyrazino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione,

(6R,12aR)-2,3,6,7,12,12a-hexahydro-2-cyclopentyl-6-(3,4-methylenedioxy phenyl)-pyrazino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione,

(6R,12aR)-2,3,6,7,12,12a-hexahydro-2-cyclopropylmethyl-6-(4-methoxyphenyl)- pyrazino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione,

(6R,12aR)-2,3,6,7,12,12a-hexahydro-6-(3-chloro-4-methoxyphenyl)-2-methyl-py razino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione,

(6R,12aR)-2,3,6,7,12,12a-hexahydro-2-methyl-6-(3,4-methylenedioxyphenyl)-py razino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione,

(6R,12aR)-2,3,6,7,12,12a-hexahydro-6-(3,4-methylenedioxyphenyl)-pyrazino[2' ,1':6,1]pyrido[3,4-b]indole-1,4-dione,

(5aR,12R,14aS)-1,2,3,5,6,11,12,14a-octahydro-12-(3,4-methylenedioxyphenyl)- pyrrolo[1",2":4',5']pyrazino[2',1':6,1]pyrido[3,4-b]indole-5-1,4-dione, and the pharmaceutically acceptable salts thereof.



41. A method as defined in claim 1 wherein said compound of said formulae (XA) or (XB) is selected from:

5-{5-[4-(2-hydroxyethyl)piperazin-1-ylsulfonyl]-2-n-propoxyphenyl}-3-n-prop yl-1-(pyridin-2-yl)methyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one,

1-(1-methylimidazol-2-yl)methyl-5-[5-(4-methylpiperazin-1-ylsulfonyl)-2-n-p ropoxyphenyl]-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one,

5-{5-[4-(2-hydroxyethyl)piperazin-1-ylsulfonyl]-2-n-propoxyphenyl}-3-n-prop yl-2-(pyridin-2-yl)methyl-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one,

5-[5-(4-ethylpiperazin-1-ylsulfonyl)-2-n-propoxyphenyl]-3-n-propyl-2-(pyrid in-2-yl)methyl-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one,

3-ethyl-5-[5-(4-ethylpiperazin-1-ylsulfonyl)-2-n-propoxyphenyl]-2-(pyridin- 2-yl)methyl-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one,

5-[5-(4-ethylpiperazin-1-ylsulfonyl)-2-n-propoxyphenyl]-3-n-propyl-2-(pyrid azin-3-yl)methyl-2,6-dihydro-7H-pyrazolo[4,3-d]pyrmidin-7-one,

5-[5-(4-ethylpiperazin-1-ylsulfonyl)-2-n-propoxyphenyl]-3-n-propyl-2-(pyrid azin-2-yl)methyl-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one,

5-[2-ethoxy-5-(4-ethylpiperazin-1-ylsulfonyl)phenyl]-3-n-propyl-2-(pyridin- 2-yl)methyl-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one, and the pharmaceutically acceptable salts thereof.



42. A method of preventing nitrate-induced tolerance in a mammal comprising administering to said mammal a nitrate-induced tolerance preventing amount of a cGMP PDE inhibitor.

Description:

FIELD OF THE INVENTION

The present invention relates to the use of certain pyrazolo[4,3-d]pyrimidin-7-ones, pyrazolo[3,4-d]pyrimidin-4-ones, quinazolin-4-ones, purin-6-ones, pyrido[3,2-d]pyrimidin-4-ones and tetracyclic derivatives to treat nitrate-induced tolerance.

BACKGROUND OF THE INVENTION

Organic nitrate esters such as, for example, glyceryl trinitrate, commonly referred to as "nitroglycerin," are well known antihypertensive agents. Administration of organic nitrate esters results in, for example, the relaxation of vascular smooth muscle. Patients having hypertension, angina pectoris, congestive heart disease, myocardial infarction, peripheral vascular disease and airways diseases often receive ongoing nitrate therapy.

It is well known that the magnitude and duration of the desired activities of nitrates diminish on chronic, continuous dosing of nitrates. This diminished activity is commonly referred to as "nitrate tolerance." While nitrate tolerance can often be avoided or reduced by intermittent versus chronic, continuous dosing, undesirable events, e.g., "rebound angina," may occur during such nitrate-free periods.

Accordingly, nitrate-induced tolerance diminishes the efficacy of the nitrate therapy, and increased doses of organic nitrate esters are often administered to provide the desired therapeutic and pharmacological effects. Efforts have been made to reduce or reverse nitrate-induced tolerance by determining, for example, how the effects of organic nitrate esters are mediated on a cellular level.

On a cellular level, cyclic guanosine 3',5'-monophosphate ("cGMP") is thought to be the second messenger through which the vascular and other effects of organic nitrate esters are mediated. Briefly, cGMP is formed from guanosine 5'-triphosphate by the enzyme guanosine 5'-triphosphate pyrophosphate ("guanylate cyclase"). The termination of cGMP action is catalyzed by cyclic nucleotide phosphodiesterases ("PDEs") which cause the opening of a 3',5'-cyclic phosphoester bond yielding 5'-cGMP.

Organic nitrate esters are known to activate guanylate cyclase leading to increased cGMP levels, and tolerance to nitrates is associated with a reduced ability to generate cGMP. Nitrate-induced increased cGMP levels can be maintained either through less degradation of existing cGMP or by increased synthesis of cGMP. For example, inhibitors of cGMP-specific cyclic nucleotide PDEs can be used to block the termination of cGMP action by maintaining cGMP levels, e.g., provided by organic nitrate ester activation of guanylate cyclase.

Reversal of nitroglycerin tolerance in vitro by a cGMP PDE inhibitor, i.e., zaprinast (also known as "M&B 22,948"), has been described in articles by: P. J. Silver et al. published in the European Journal of Pharmacology, Vol. 199 (1): pp. 141-142 (1991), T. L. G. Anderson et al. published in the Journal of Cardiovascular Pharmacology, Vol. 18 (2): pp. 237-242 (1991), L. A. Merkel et al. published in the European Journal of Pharmacology, Vol. 216 (1): pp. 29-35 (1992), L. De Garavilla et al. published in the Journal of Molecular and Cellular Cardiology, Vol. 24 (Suppl. 3): S37 (1992) and in the European Journal of Pharmacology, Vol. 313 (1-2): pp. 89-96 (1996), and by E. D. Pagani et al. published in the European Journal of Pharmacology, Vol. 243 (2): pp. 141-7 (1993).

Synergism of a cGMP PDE inhibitor, i.e., E4021, with nitroglycerin, has been described in an article by T. Saeki et al. published in the Journal of Pharmacology and Experimental Therapeutics, Vol. 272 (2): pp. 825-831 (1995) (an increase in cGMP levels and a relaxant effect in isolated porcine coronary artery).

Reversal of nitroglycerin tolerance in vitro by a cGMP PDE inhibitor, i.e., cicletanine, has been described in an article by Z. Szilvassy et al. published in the Journal of Molecular and Cellular Cardiology, Vol. 28 (5): A97 (1996).

U.S. Pat. No. 5,294,612 discloses 6-heterocyclyl-pyrazolo[3,4-d]pyrimidin-4-ones possessing cGMP PDE I inhibitory activity, and the use of such compounds in combination with nitrates to reverse and/or reduce nitrate-induced tolerance.

U.S. Pat. No. 5,488,055 and International PCT Application published as WO 96/28446 disclose substituted N-cycloalkylmethyl-1H-pyrazolo[3,4-b]quinolin-4-amines possessing c-GMP PDE V inhibitory activity, and the use of such compounds in combination with nitrates to reverse and/or reduce nitrate-induced tolerance.

U.S. Pat. No. 5,541,187, a division of the aforementioned U.S. Pat. No. 5,294,612, discloses 6-heterocyclyl-pyrazolo[3,4-d]pyrimidin-4-ones possessing cGMP PDE I inhibitory activity, and the use of such compounds in combination with nitrates to reverse and/or reduce nitrate-induced tolerance.

U.S. Pat. No. 5,614,530 and International PCT Application published as WO 96/128159 disclose substituted N-arylmethyl and heterocyclylmethyl-1H-pyrazolo[3,4-b]quinolin-4-amines possessing c-GMP PDE V inhibitory activity, and the use of such compounds in combination with nitrates to reverse and/or reduce nitrate-induced tolerance.

U.S. Pat. No. 5,656,629 and International PCT Application published as WO 96/28429 disclose 6-substituted pyrazolo[3,4-d]pyrimidin-4-one derivatives possessing c-GMP PDE V inhibitory activity, and the use of such compounds in combination with nitrates to reverse and/or reduce nitrate-induced tolerance.

U.S. Pat. No. 5,736,548 and International PCT Application published as WO 96/28448 disclose 6-arylpyrazolo[3,4-d]pyrimidin-4-one derivatives possessing c-GMP PDE V inhibitory activity, and the use of such compounds in combination with nitrates to reverse and/or reduce nitrate-induced tolerance.

U.S. Pat. Nos. 5,250,534, 5,272,147, and 5,346,901, a division of the aforementioned U.S. Pat. No. 5,250,534, and International PCT Applications published as WO 93/06104, WO 93/07149, WO 94/28902 and WO 98/49166, disclose pyrazolo[4,3-d]pyrimidinones possessing cGMP PDE inhibitory activity.

U.S. Pat. No. 5,734,053 and International PCT Application published as WO 94/00453 disclose purinones possessing cGMP PDE inhibitory activity.

U.S. Pat. No. 5,482,941 and International PCT Application published as WO 93/12095 disclose quinazolinones possessing cGMP PDE inhibitory activity.

U.S. Pat. No. 5,591,742 and International PCT Application published as WO 94/05661 disclose pyridopyrimidinones possessing cGMP PDE inhibitory activity.

International PCT Application published as WO 96/16657 discloses 5-arylpyrazolo[4,3-d]pyrimidin-7-ones, 6-arylpyrazolo[3,4-d]pyrimidin-4-ones, 2-arylquinazolin-4-ones, 2-arylpurin-6-ones and 2-arylpyrido[3,2-d]pyrimidin-4-ones possessing cGMP PDE inhibitory activity.

International PCT Application published as WO 95/19978 discloses tetracyclic derivatives possessing cGMP PDE inhibitory activity. International PCT application published as WO 97/03675 discloses the use of such tetracyclic derivatives to treat impotence.

The present invention relates to the use of certain pyrazolo[4,3-d]pyrimidin-7-ones, pyrazolo[3,4-d]pyrimidin-4-ones, quinazolin-4-ones, purin-6-ones, pyrido[3,2-d]pyrimidin-4-ones and tetracyclic derivatives for the treatment of nitrate-induced tolerance.

All of the documents cited herein, including the foregoing, are incorporated by reference herein in their entireties.

SUMMARY OF THE INVENTION

The present invention relates to certain pyrazolo[4,3-d]pyrimidin-7-ones, pyrazolo[3,4-d]pyrimidin-4-ones, quinazolin-4-ones, purin-6-ones, pyrido[3,2d]pyrimidin-4-ones or tetracyclic derivatives, and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof, which are useful in the treatment of nitrate-induced tolerance.

Specifically, suitable compounds include those which are disclosed in the aforementioned U.S. Pat. Nos. 5,250,534, 5,272,147, 5,346,901, 5,734,053, 5,482,941 and 5,591,742 and the International PCT Applications published as WO 93/06104, WO 93/07149, WO 93/12095, WO 94/00453, WO 94/05661, WO 94/28902, WO 96/16657, WO 95/19978; WO 97/03675; and WO 98/49166.

Thus, the present invention provides methods of treating nitrate-induced tolerance in a mammal which comprise administering to said mammal a nitrate-tolerance treating amount of a compound of formulae (I), (II), (III), (IV), (V), (VI), (VII), (VIII), (IX), (XA) or (XB) herein, or the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites or stereoisomers thereof.

Also provided by the present invention are pharmaceutical compositions for the treatment of nitrate-induced tolerance comprising a nitrate-induced tolerance treating amount of a compound of formulae (I), (II), (III), (IV), (V), (VI), (VII), (VIII), (IX), (XA) or (XB) herein, or the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites or stereoisomers thereof, and a pharmaceutically acceptable vehicle, diluent or carrier.

In a first aspect of the present invention the compound of the novel methods and pharmaceutical compositions for treating nitrate-induced tolerance is selected from those which are disclosed in the aforementioned U.S. Pat. No. 5,250,534, including, for example, the compounds of formula (I) below: ##STR1##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R 1 is H, C 1 -C 3 alkyl, C 3 -C 5 cycloalkyl or C 1 -C 3 perfluoroalkyl;

R 2 is H, C 1 -C 6 alkyl optionally substituted by OH, C 1 -C 3 alkoxy or C 3 -C 6 cycloalkyl, or C 1 -C 3 perfluoroalkyl;

R 3 is C 1 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, C 3 -C 7 cycloalkyl, C 1 -C 6 perfluoroalkyl or (C 3 -C 6 cycloalkyl)C 1 -C 6 alkyl;

R 4 taken together with the nitrogen atom to which it is attached completes a 4-N--(R 6 )-piperazinyl group;

R 5 is H, C 1 -C 4 alkyl, C 1 -C 3 alkoxy, NR 7 R 8 or CONR 7 R 8 ;

R 6 is H, C 1 -C 6 alkyl, (C 1 -C 3 alkoxy)C 2 -C 6 alkyl, hydroxy C 2 -C 6 alkyl, (R 7 R 8 N)C 2 -C 6 alkyl, (R 7 R 8 NCO)C 1 -C 6 alkyl, CONR 7 R 8 , CSNR 7 R 8 or C(NH)NR 7 R 8 ; and

R 7 and R 8 are each independently H, C 1 -C 4 alkyl, (C 1 -C 3 alkoxy)C 2 -C 4 alkyl or hydroxy C 2 -C 4 alkyl.

In a second aspect of the present invention the compound of the novel methods and pharmaceutical compositions for treating nitrate-induced tolerance is selected from those which are disclosed in the aforementioned U.S. Pat. No. 5,272,147 including, for example, the compounds of formula (II) below: ##STR2##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R 9 is H, C 1 -C 3 alkyl optionally substituted with one or more fluoro substituents, or C 3 -C 5 cycloalkyl;

R 10 is H or C 1 -C 6 alkyl optionally substituted with one or more fluoro substituents or with C 3 -C 6 cycloalkyl;

R 11 is C 1 -C 6 alkyl optionally substituted with one or more fluoro substituents or with C 3 -C 6 cycloalkyl, or C 3 -C 5 cycloalkyl, or C 3 -C 6 alkenyl, or C 3 -C 6 alkynyl;

R 12 is C 1 -C 4 alkyl optionally substituted with OH, NR 13 R 14 , CN, CONR 13 R 14 or with CO 2 R 15 , or C 2 -C 4 alkenyl optionally substituted with CN, CONR 13 R 14 or with CO 2 R 15 , or C 2 -C 4 alkanoyl optionally substituted with NR 13 R 14 , or hydroxy C 2 -C 4 alky optionally substituted with NR 13 R 14 , or (C 2 -C 3 alkoxy)C 1 -C 2 alkyl optionally substituted with OH or NR 13 R 14 , or CONR 13 R 14 , or CO 2 R 15 , or halo, or NR 13 R 14 , or NHSO 2 NR 13 R 14 , or NHSO 2 R 16 , or phenyl or heterocyclyl either of which is optionally substituted with methyl;

R 13 and R 14 are each independently H, C 1 -C 4 alkyl, or together with the nitrogen atom to which they are attached form a pyrrolidinyl, piperidino, morpholino, 4-(NR 17 )-piperazinyl or imidazolyl group wherein said group is optionally substituted with methyl or hydroxy;

R 15 is H or C 1 -C 4 alkyl;

R 16 is C 1 -C 3 alkyl optionally substituted with NR 13 R 14 ; and

R 17 is H, C 1 -C 3 alkyl optionally substituted with phenyl, or hydroxy C 2 -C 3 alkyl, or C 1 -C 4 alkanoyl.

In a third aspect of the present invention the compound of the novel methods and pharmaceutical compositions for treating nitrate-induced tolerance is selected from those which are disclosed in the aforementioned U.S. Pat. No. 5,346,901 including, for example, the compounds of formula (III) below: ##STR3##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein: R 4 , R 2 , R 3 and R 5 are as previously described for formula (I) herein, and R 18 taken together with the nitrogen to which it is attached completes a pyrrolidinyl, piperidino or morpholino group.

In a fourth aspect of the present invention the compound of the novel methods and pharmaceutical compositions for treating nitrate-induced tolerance is selected from those which are disclosed in the aforementioned U.S. Pat. No. 5,734,053 and International PCT Application published as WO 94/00453, including, for example, the compounds of formula (IV) below: ##STR4##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R 19 is C 1 -C 4 alkyl;

R 20 is C 2 -C 4 alkyl;

R 21 is H or SO 2 NR 22 R 23 ;

R 22 and R 23 together with the nitrogen atom to which they are attached form a pyrrolidino, piperidino, morpholino or 4-N--(R 24 )-1-piperazinyl group; and

R 24 is H or C 1 -C 3 alkyl.

In a fifth aspect of the present invention the compound of the novel methods and pharmaceutical compositions for treating nitrate-induced tolerance is selected from those which are disclosed in the aforementioned U.S. Pat. No. 5,482,941 and International PCT Application published as WO 93/12095, including, for example, the compounds of formula (V) below: ##STR5##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R 25 is H, C 1 -C 4 alkyl, C 1 -C 4 alkoxy or CONR 29 R 30 ;

R 26 is H or C 1 -C 4 alkyl;

R 27 is C 2 -C 4 alkyl;

R 28 is H, C 2 -C 4 alkanoyl optionally substituted with NR 31 R 32 , or (hydroxy)C 2 -C 4 alkyl optionally substituted with NR 31 R 32 , or CHCHCO 2 R 33 , or CHCHCONR 31 R 32 , or CH 2 CH 2 CO 2 R 33 , or CH 2 CH 2 CONR 31 R 32 , or SO 2 NR 31 R 32 , or SO 2 NH(CH 2 ) n NR 31 R 32 or imidazolyl;

R 29 and R 30 are each independently H or C 1 -C 4 alkyl;

R 31 and R 32 are each independently H or C 1 -C 4 alkyl, or together with the nitrogen atom to which they are attached form a pyrrolidino, piperidino, morpholino or 4-(NR 34 )-1-piperazinyl group wherein any of said groups is optionally substituted with CONR 29 R 30 ;

R 33 is H or C 1 -C 4 alkyl;

R 34 is H, C 1 -C 3 alkyl or (hydroxy)C 2 -C 3 alkyl; and

n is 2, 3 or 4; and provided that R 28 is not H when R 25 is H, C 1 -C 4 alkyl or C 1 -C 4 alkoxy.

In a sixth aspect of the present invention the compound of the novel methods and pharmaceutical compositions for treating nitrate-induced tolerance is selected from those which are disclosed in the aforementioned U.S. Pat. No. 5,591,742 and International PCT Application published as WO 94/05661, including, for example, the compounds of formula (VI) below: ##STR6##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R 35 is H, C 1 -C 4 alkyl, CN or CONR 29 R 30 ;

R 36 is C 2 -C 4 alkyl;

R 37 is SO 2 NR 38 R 39 , NO 2 , NH 2 , NHCOR 42 , NHSO 2 R 42 or N(SO 2 R 42 ) 2 ;

R 38 and R 39 are each independently selected from H and C 1 -C 4 alkyl optionally substituted with CO 2 R 43 , OH, pyridyl, 5-isoxazolin-3-onyl, morpholino or 1-imidazolidin-2-onyl, or together with the nitrogen atom to which they are attached form a pyrrolidino, piperidino, morpholino, 1-pyrazolyl or 4-(NR 44 )-1-piperazinyl group wherein any of said groups may optionally be substituted with one or two substituents selected from C 1 -C 4 alkyl, CO 2 R 43 , NH 2 and OH;

R 42 is C 1 -C 4 alkyl or pyridyl;

R 43 is H or C 1 -C 4 alkyl; and

R 44 is H, C 1 -C 4 alkyl or (hydroxy)C 2 -C 3 alkyl.

In a seventh aspect of the present invention the compound of the novel methods and pharmaceutical compositions for treating nitrate-induced tolerance is selected from those which are disclosed in the aforementioned International PCT Application published as WO 93/07149, including, for example, the compounds of formula (VII) below: ##STR7##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R 45 is C 1 -C 6 alkyl;

R 46 is H, methyl or ethyl;

R 47 is C 2 -C 4 alkyl;

R 48 is C 1 -C 4 alkyl optionally substituted with NR 49 R 50 , CN, CONR 49 R 50 or CO 2 R 51 ; C 2 -C 4 alkenyl optionally substituted with CN, CONR 49 R 50 or CO 2 R 51 ; C 2 -C 4 alkanoyl optionally substituted with NR 49 R 50 ; SO 2 NR 49 R 50 ; CONR 49 R 50 ; CO 2 R 51 ; or halo;

R 49 and R 50 are each independently H or C 1 -C 4 alkyl, or together with the nitrogen atom to which they are attached form a pyrrolidino, piperidino, morpholino, 4-(NR 52 )-1-piperazinyl or 1-imidazolyl group wherein said group is optionally substituted by one or two C 1 -C 4 alkyl groups;

R 51 is H or C 1 -C 4 alkyl; and

R 52 is H, C 1 -C 3 alkyl or hydroxy C 2 -C 3 alkyl.

In an eighth aspect of the present invention the compound of the novel methods and pharmaceutical compositions for treating nitrate-induced tolerance is selected from those which are disclosed in the aforementioned International PCT Application published as WO 93/06104, including, for example, the compounds of formula (VIII) below: ##STR8##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R 53 is methyl or ethyl;

R 54 is ethyl or n-propyl;

R 55 and R 56 are each independently H or C 1 -C 6 alkyl optionally substituted with C 5 -C 7 cycloalkyl or with morpholino.

In a ninth aspect of the present invention the compound of the novel methods and pharmaceutical compositions for treating nitrate-induced tolerance is selected from those which are disclosed in the aforementioned International PCT Applications published as WO 95/19978 and WO 97/03675, including, for example, the compounds of formula (IX) below: ##STR9##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R 57 is hydrogen, halogen or C 1 -6 alkyl;

R 58 is hydrogen, C 1 -6 alkyl, C 2 -6 alkenyl, C 2 -6 alkynyl, halo C 1 -6 alkyl, C 3 -8 cycloalkyl, C 3 -8 cycloalkyl C 1 -3 alkyl, aryl C 1 -3 alkyl or heteroaryl C 1 -3 alkyl;

R 59 is an optionally substituted monocyclic aromatic ring selected from benzene, thiophene, furan and pyridine or an optionally substituted bicyclic ring ##STR10##

attached to the rest of the molecule via one of the benzene ring carbon atoms and wherein the fused ring A is a 5- or 6-membered ring which may be saturated or partially or fully unsaturated and comprises carbon atoms and optionally one or two heteroatoms selected from oxygen, sulfur and nitrogen; and

R 60 is hydrogen or C 1 -3 alkyl, or R 58 and R 60 together represent a 3- or 4-membered alkyl or alkenyl chain.

In a tenth aspect of the present invention the compound of the novel methods and pharmaceutical compositions for treating nitrate-induced tolerance is selected from those which are disclosed in the aforementioned International PCT Application published as WO 98/49166 including, for example, the compounds of formulae (XA) and (XB) below: ##STR11##

and the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites and stereoisomers thereof; wherein:

R 61 is C 1 -C 3 alkyl substituted with C 3 -C 6 cycloalkyl, CONR 55 R 66 or a N-linked heterocyclic group selected from pyrazolyl, imidazolyl, triazolyl, pyrrolidinyl, piperidinyl, morpholinyl and 4-R 67 -piperazinyl; (CH 2 ) p Het or (CH 2 ) q Ar;

R 62 is C 1 -C 6 alkyl;

R 63 is C 1 -C 6 alkyl optionally substituted with C 1 -C 4 alkoxy;

R 64 is SO 2 NR 68 R 69 ;

R 65 and R 66 are each independently selected from H and C 1 -C 4 alkyl optionally substituted with C 1 -C 4 alkoxy, or, together with the nitrogen atom to which they are attached, form a pyrrolidinyl, piperidinyl, morpholinyl or 4-R 67 -piperazinyl group;

R 68 and R 69 , together with the nitrogen atom to which they are attached, form a 4-R 70 -piperazinyl group;

R 67 is C 1 -C 4 alkyl;

R 70 is H or C 1 -C 4 alkyl optionally substituted with OH, C 1 -C 4 alkoxy or CONH 2 ;

Het is a C-linked 6-membered heterocyclic group containing one or two nitrogen atoms, optionally in the form of its mono-N-oxide, or a C-linked 5-membered ring heterocyclic group containing from one to four heteroatoms selected from nitrogen, oxygen and sulfur, wherein either of said heterocyclic groups is optionally substituted with one or two substituents selected from C 1 -C 4 alkyl optionally substituted with C 1 -C 4 alkoxy, C 1 -C 4 alkoxy, halo and NH 2 ;

Ar is phenyl optionally substituted with one or two substituents selected from C 1 -C 4 alkyl, C 1 -C 4 alkoxy, halo, CN, CONH 2 , NO 2 , NH 2 , NHSO 2 (C 1 -C 4 alkyl) and SO 2 NH 2 ; and

p and q are each independently 0 or 1.

In an eleventh aspect, the present invention provides a method for preventing nitrate-induced tolerance in a mammal comprising administering to such mammal a nitrate-induced tolerance preventing amount of a cGMP PDE inhibitor.

Any suitable nitric oxide inhibitor, e.g., organic nitrate, i.e., polyol ester of nitric acid (--C--O--NO 2 ), may be used in the novel methods of the present invention. Suitable organic nitrates include, for example, those of low, e.g., glyceryl trinitrate, and high, e.g., erythrityl tetranitrate, pentaerythritol tetranitrate and isosorbide dinitrate, molecular mass. Preferred organic nitrates include glyceryl trinitrate.

DETAILED DESCRIPTION OF THE INVENTION

Those skilled in the art will fully understand the terms used herein to describe the compounds comprising the novel methods and pharmaceutical compositions; nonetheless, the following terms used herein, unless otherwise provided by the aforementioned U.S. Pat. Nos. 5,250,534; 5,272,147; 5,346,901; 5,734,053; 5,482,941; and 5,591,742, and the International PCT Applications published as WO 93/06104; WO 93/07149; WO 93/12095; WO 94/00453; WO 94/05661; WO 94/28902; WO 96/16657; WO 95/19978; WO 97/03675 and WO 98/49166, are as described below.

"Alkanoyl" means a univalent or bivalent acyl radical formed by removal of hydroxyl from the carboxyl group which replaced the methyl group at the end of the main chain of the acyclic hydrocarbon.

"Alkenyl" means an unsaturated, unbranched acyclic hydrocarbon radical having one double bond.

"Alkoxy" means an alkyl radical attached to the remainder of the molecule by oxygen, including, for example, methoxy.

"Alkyl" means a straight or branched hydrocarbon chain radical, including, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl and the like.

"Alkynyl" means an unsaturated, unbranched acyclic hydrocarbon radical having one triple bond, including, for example, acetylene.

"Allyl" means prop-2-enyl, i.e., the radical --CH 2 CHCH 2 .

"Aryl" means an organic radical derived from an aromatic hydrocarbon by the removal of one atom, e.g., phenyl from benzene, also including, for example, naphthyl.

"Cycloalkane" means a saturated, monocyclic hydrocarbon, including, for example, cyclohexane.

"Cycloalkyl" means a monocyclic or polycyclic radical derived from a cycloalkane, including, for example, cyclohexyl, cyclobutyl, cyclopentyl and cycloheptyl.

"Halo" or "halogen" means a radical derived from the elements fluorine, chlorine, bromine and iodine.

"Heterocyclyl" means a radical derived from a ring of different types of atoms, and includes aromatic and non-aromatic heterocyclic groups containing one or more heteroatoms each selected from O, S and N. The heterocyclic groups include benzofused ring systems and ring systems substituted with an oxo moiety, e.g., benzimidazolyl, benzofuranyl, benzothiophenyl, benzoxazolyl, furyl, imidazolyl, indolyl, isoquinolyl, isothiazolyl, isoxazolyl, morpholinyl, oxadiazolyl, oxazolyl, piperazinyl, piperidyl, pyrazinyl, pyrazolyl, pyridyl, pyrimidyl, pyrrolyl, quinolyl, tetrahydroisoquinoly, tetrahydroquinolyl, tetrahydrothienyl, tetrazolyl, thiadiazolyl, thiazolyl, thienyl, thiomorpholinyl and triazolyl. Where heterocyclic groups are specifically recited or covered as substituents for the compounds of formulae (I)-(XB), it is understood that all suitable isomers of such heterocyclic groups are intended.

"Perfluoroalkyl" means that all of the H atoms, except those whose replacement would affect the nature of the characteristic groups present, are replaced with fluorine atoms, e.g., perfluoropentyl, CF 3 (CF 2 ) 3 CF 2 --.

"Pharmaceutically acceptable salt(s)" includes salts of acidic or basic groups which may be present in the compounds suitable for use in the present invention, e.g., the compounds of formulae (I)-(XB) herein. For example, pharmaceutically acceptable salts include sodium, calcium and potassium salts of carboxylic acid groups and hydrochloride salts of amino groups. Other pharmaceutically acceptable salts of amino groups are hydrobromide, sulfate, hydrogen sulfate, phosphate, hydrogen phosphate, dihydrogen phosphate, acetate, succinate, citrate, tartrate, lactate, mandelate, methanesulfonate (mesylate) and p-toluenesulfonate (tosylate) salts. A preferred salt is the citrate.

"Treating," "treat" or "treatment" includes, inter alia, preventative (e.g., prophylactic), palliative and curative treatment, including, for example, the prevention, reduction and reversal of nitrate-induced tolerance.

As disclosed herein, a compound within the scope of formulae (I)-(XB), shall at all times be understood to include all active forms of such compounds, including, for example, the free form thereof, e.g., the free acid or base form and also, all pharmaceutically acceptable salts as described above, prodrugs, polymorphs, hydrates, solvates, stereoisomers, e.g., diastereomers and enantiomers, and the like. It will also be appreciated that active metabolites of compounds within the scope of formulae (I)-(XB), in any suitable form, are also included herein.

More specifically, certain compounds suitable for use in the present invention such as, for example, certain compounds of formulae (I)-(XB), may have asymmetric centers and therefore exist in different enantiomeric forms. All optical isomers and stereoisomers of such compounds, and mixtures thereof, are considered to be within the scope of the invention. With respect to such compounds, the present invention includes the use of a racemate, a single enantiomeric form, a single diastereomeric form, or mixtures thereof. Moreover, such compounds may also exist as tautomers. Accordingly, the present invention relates to the use of all such tautomers and mixtures thereof. Any suitable combination of any of the compounds of formulae (I)-(XB) herein, or the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites or stereoisomers thereof, may be used in the methods and pharmaceutical compositions of the present invention.

The preparation of the compounds suitable for use in the present invention including the compounds of formulae (I)-(XB) herein, and their pharmaceutically acceptable salts, and the preferred compounds thereof, pharmaceutical compositions thereof and routes of administration for mammalian use, can be understood and carried out by one skilled in the art in any suitable manner, e.g., according to one or more of the synthetic methods outlined in the synthetic schemes and examples described in considerable detail in the aforementioned U.S. Pat. Nos. 5,250,534; 5,272,147; 5,346,901; 5,734,053; 5,482,941 and 5,591,742, and the International PCT Applications published as WO 93/06104; WO 93/07149; WO 93/12095; WO 94/00453; WO 94/05661; WO 94/28902; WO 96/16657; WO 95/19978; WO 97/03675; and WO 98/49166.

Preferred compounds of formula (I) include those wherein R 1 is H, methyl or ethyl; R 2 is C 1 -C 3 alkyl optionally substituted by OH or methoxy; R 3 is C 2 -C 3 alkyl or allyl; R 4 taken together with the nitrogen atom to which it is attached completes a piperidino or 4-N--(R 6 )-piperazinyl group; R 5 is H, NR 7 R 8 or CONR 7 R 8 ; R 6 is H, C 1 -C 3 alkyl, hydroxy C 2 -C 3 alkyl, CONR 7 R 8 , CSNR 7 R 8 or C(NH)NR 7 R 8 ; and R 7 and R 8 are each independently H or methyl.

Other preferred compounds of formula (I) include those wherein R 1 is methyl; R 2 is n-propyl; R 3 is ethyl, n-propyl or allyl; R 4 taken together with the nitrogen atom to which it is attached completes a 4-N--(R 6 )-piperazinyl group; R 5 is H; R 6 is H, C 1 -C 3 alkyl or 2-hydroxyethyl; and R 7 and R 8 are each independently H or methyl.

A further preferred compound of formula (I) is wherein R 1 is methyl, R 2 is n-propyl, R 3 is ethyl, R 4 taken together with the nitrogen atom to which it is attached completes a 4-N--(R 6 )-piperazinyl group, R 5 is hydrogen and R 6 is methyl.

Also preferred is the citrate salt of a compound of formula (I) wherein R 1 is methyl, R 2 is n-propyl, R 3 is ethyl, R 4 taken together with the nitrogen atom to which it is attached completes a 4-N--(R 6 )-piperazinyl group, R 5 is hydrogen and R 6 is methyl.

Preferred individual compounds of formula (I) include:

5-[2-allyloxy-5-(4-methylpiperazinylsulphonyl)phenyl]-1-meth yl-3-n-propyl-1 ,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one;

5-[2-ethoxy-5-(piperazinylsulphonyl)phenyl]-1-methyl-3-n-pro pyl-1,6-dihydro -7H-pyrazolo[4,3-d]pyrimidin-7-one;

5-[2-ethoxy-5-(4-methylpiperazinylsulphonyl)phenyl]-1-methyl -3-n-propyl-1,6 -dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one;

5-{2-ethoxy-5-[4-(2-propyl)piperazinylsulphonyl]phenyl}-1-me thyl-3-n-propyl -1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one;

5-{2-ethoxy-5-[4-(2-hydroxyethyl)piperazinylsulphonyl]phenyl }-1-methyl-3-n- propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one;

1-methyl-5-[5-piperazinylsulphonyl)-2-n-propoxy-phenyl]-3-n- propyl-1,6-dihy dro-7H-pyrazolo[4,3-d]pyrimidin-7-one; and

5-{5-[4-(2-hydroxyethyl)piperazinyisulphonyl]-2-n-propoxyphe nyl}-1-methyl-3 -n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one.

Preferred compounds of formula (II) include those wherein R 9 is H, methyl or ethyl; R 10 is C 1 -C 3 alkyl; R 11 is C 2 -C 3 alkyl; R 12 is C 1 -C 2 alkyl optionally substituted with OH, NR 13 R 14 , CONR 13 R 14 or with CO 2 R 15 , acetyl optionally substituted with NR 13 R 14 , or hydroxyethyl substituted with NR 13 R 14 , or ethoxymethyl optionally substituted with OH or with NR 13 R 14 , or CHCHCN, or CHCHCONR 13 R 14 , or CHCHCO 2 R 15 , or CO 2 H, or CONR 13 R 14 , or Br, or NR 13 R 14 , or NHSO 2 NR 13 R 14 , or NHSO 2 R 16 , or pyridinyl or imidazolyl either of which is optionally substituted with methyl; R 13 and R 14 are each independently H, methyl or ethyl, or together with the nitrogen atom to which they are attached form a piperidino, morpholino, 4-(NR 17 )-1-piperazinyl or imidazolyl group wherein said group is optionally substituted with methyl or hydroxy; R 15 is H or t-butyl; R 16 is methyl or CH 2 CH 2 CH 2 NR 13 R 14 ; and R 17 is H, methyl, benzyl, 2-hydroxyethyl or acetyl.

Other preferred compounds of formula (II) include those wherein R 9 is methyl; R 10 is n-propyl; R 11 is ethyl or n-propyl; R 12 is CH 2 NR 13 R 14 , CH 2 OCH 2 CH 2 NR 13 R 14 , CH 2 OCH 2 CH 3 , CH 2 OCH 2 CH 2 OH, COCH 2 NR 13 R 14 , CH(OH)CH 2 NR 13 R 14 , CHCHCON(CH 3 ) 2 , CHCHCO 2 R 15 , CO 2 H, CONR 13 R 14 , Br, NHSO 2 NR 13 R 14 , NHSO 2 CH 2 CH 2 CH 2 NR 13 R 14 , 2-pyridyl, 1-imidazolyl or 1-methyl-2-imidazolyl; R 13 and R 14 together with the nitrogen atom to which they are attached form a piperidino, 4-hydroxypiperidino, morpholino, 4-(NR 17 )-1-piperazinyl or 2-methyl-1-imidazolyl group; R 15 is H or t-butyl; R 16 is methyl or CH 2 CH 2 CH 2 NR 13 R 14 ; and R 17 is H, methyl, benzyl, 2-hydroxyethyl or acetyl.

Preferred individual compounds of formula (II) include:

5-[2-ethoxy-5-(1-methyl-2-imidazolyl)phenyl]-1-methyl-3-n-pr opyl-1,6-dihydr o-7H-pyrazolo[4,3-d]pyrimidin-7-one;

5-[2-ethoxy-5-(4-methyl-1-piperazinylcarbonyl)phenyl]-1-meth yl-3-n-propyl-1 ,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one;

5-[5-(4-acetyl-1-piperazinyl)acetyl-2-ethoxyphenyl]-1-methyl -3-n-propyl-1,6 -dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one;

5-(2-ethoxy-5-morpholinoacetylphenyl)-1-methyl-3-n-propyl-1, 6-dihydro-7H-py razolo[4,3-d]pyrimidin-7-one; and

5-(5-morpholinoacetyl-2-propoxyphenyl)-1-methyl-3-n-propyl-1 ,6-dihydro-7H-p yrazolo[4,3-d]pyrimidin-7-one.

Preferred compounds of formula (III) include those wherein R 4 is H, methyl or ethyl; R 2 is C 1 -C 3 alkyl optionally substituted by OH or methoxy; R 3 is C 2 -C 3 alkyl or allyl; R 18 taken together with the nitrogen atom to which it is attached completes a piperidino group; R 5 is H, NR 7 R 8 or CONR 7 R 8 ; and R 7 and R 8 are each independently H or methyl.

Preferred compounds of formula (IV) include those wherein R 19 and R 20 are each independently ethyl or n-propyl; and R 22 and R 23 together with the nitrogen atom to which they are attached form a 4-N--(R 24 )-1-piperazinyl group.

Other preferred compounds of formula (IV) include those wherein R 19 is n-propyl; R 20 is ethyl; and R 21 is 1-piperazinylsulphonyl or 4-methyl-1-piperazinylsulfonyl.

Preferred compounds of formula (V) include those wherein R 25 is H, methoxy or CONR 29 R 30 ; R 26 is H or methyl; R 27 is ethyl or n-propyl; R 28 is H, acetyl optionally substituted with NR 31 R 32 , or hydroxyethyl substituted with NR 31 R 32 , or CHCHCO 2 R 32 , or CHCHCONR 31 R 32 , or CH 2 CH 2 CO 2 R 33 , or SO 2 NR 31 R 32 , or SO 2 NH(CH 2 ) 3 NR 31 R 32 or 1-imidazolyl; R 29 and R 30 are each independently H or ethyl; R 31 and R 32 together with the nitrogen atom to which they are attached form a piperidino, 4-carbamoylpiperidino, morpholino or 4-(NR 34 )-1-piperazinyl group; R 33 is H or t-butyl; and R 34 is H, methyl or 2-hydroxyethyl; provided that R 28 is not H when R 25 is H, methyl or methoxy.

Other preferred compounds of formula (V) include those wherein R 25 is methyl, CONH 2 or CONHCH 2 CH 3 ; R 26 is H; R 27 is ethyl or n-propyl; R 28 is H, acetyl, 1-hydroxy-2-(NR 31 R 32 )ethyl, CHCHCO 2 C(CH 3 ) 3 , or CHCHCONR 31 R 32 , or SO 2 NR 31 R 32 or 1-imidazolyl; R 31 and R 32 together with the nitrogen atom to which they are attached form a 4-(NR 34 )-1-piperazinyl group; and R 34 is methyl or 2-hydroxyethyl; provided that R 28 is not H when R 25 is methyl.

Preferred individual compounds of formula (V) include:

2-{2-ethoxy-5-[4-(2-hydroxyethyl)-1-piperazinylsulfonyl]phen yl}-8-methyl quinazolin-4(3H)-one;

2-{5-[4-(2-hydroxyethyl)-1-piperazinylsulfonyl]2-n-propoxyph enyl}-8-methyl quinazolin-4(3H)-one;

8-methyl-2-{5-[2-(4-methyl-1-piperazinylcarbonyl)ethenyl]-2- n-propoxy-pheny l}quinazolin-4(3H)-one;

8-carbamoyl-2-{2-ethoxy-5-[4-(2-hydroxyethyl)-1-piperazinyls ulfonyl]phenyl} quinazolin-4(3H)-one; and

8-ethylcarbamoyl-2-(2-n-propoxyphenyl)quinazolin-4(3H)-on e.

Preferred compounds of formula (VI) include those wherein R 35 is H, n-propyl, CN or CONH 2 ; R 36 is ethyl; R 37 is SO 2 NR 40 R 41 , NO 2 , NH 2 , NHCOCH(CH 3 ) 2 , NHSO 2 CH(CH 3 ) 2 , NHSO 2 (3-pyridyl) or N[SO 2 (3-pyridyl)] 2 ; R 40 is H, methyl or 2-hydroxyethyl; R 41 is methyl optionally substituted with 2-pyridyl or 5-isoxazolin-3-onyl, or ethyl 2-substituted with OH, CO 2 CH 2 CH 3 , morpholino or with 1-imidazolidin-2-onyl; or R 40 and R 41 together with the nitrogen atom to which they are attached form a (4-CO 2 R 43 )piperidino, 5-amino-3-hydroxy-1-pyrazolyl or 4-(NR 44 )-1-piperazinyl group; R 43 is H or ethyl; and R 44 is H, methyl or 2-hydroxyethyl.

Other preferred compounds of formula (VI) include those wherein R 35 is n-propyl or CN; R 36 is ethyl; R 37 is SO 2 NR 40 R 41 , NHSO 2 CH(CH 3 ) 2 , NHSO 2 (3-pyridyl) or N[SO 2 (3-pyridyl)] 2 ; R 40 is H or methyl; R 41 is methyl, ethyl 2-substituted with CO 2 CH 2 CH 3 , morpholino or 1-imidazolidin-2-onyl; or R 40 and R 41 together with the nitrogen atom to which they are attached form a (4-CO 2 R 43 )piperidino or 4-(NR 44 )-1-piperazinyl group; R 43 is H or ethyl; and R 44 is H, methyl or 2-hydroxyethyl.

Preferred individual compounds of formula (VI) include:

2-[2-ethoxy-5-(4-ethoxycarbonylpiperidinosulfonyl)phenyl]-8- n-propylpyrido [3,2-d]pyrimidin-4(3H)-one;

2-[5-(4-carboxypiperidinosulfonyl)-2-ethoxyphenyl]-8-n-propy lpyrido [3,2-d]pyrimidin-4(3H)-one;

2-{2-ethoxy-5-[4-(2-hydroxyethyl)-1-piperazinylsulfonyl]phen yl}-8-n-propyl pyrido[3,2-d]pyrimidin-4(3H)-one; and

2-{2-ethoxy-5-[(bis-3-pyridylsulfonyl)amino]phenyl}-8-n-prop ylpyrido [3,2-d]pyrimidin-4(3H)-one.

Preferred compounds of formula (VII) include those wherein R 45 is n-propyl; R 46 is H or methyl; R 47 is ethyl or n-propyl; R 48 is ethyl substituted with CONR 49 R 50 or CO 2 R 51 , vinyl substituted with CONR 49 R 50 or CO 2 R 51 , acetyl substituted with NR 49 R 50 , or SO 2 NR 49 R 50 , or CONR 49 R 50 , or CO 2 R 51 , or bromo; R 49 and R 50 together with the nitrogen atom to which they are attached form a morpholino, 4-(NR 52 )-1-piperazinyl or 2,4-dimethyl-1-imidazolyl group; R 51 is H or t-butyl; and R 52 is methyl or 2-hydroxyethyl.

Preferred individual compounds of formula (VII) include:

6-(5-bromo-2-n-propoxyphenyl)-3-methyl-1-n-propyl-1,5-dihydr o-4H-pyrazolo[3 ,4-d]pyrimidin-4-one;

3-methyl-6-(5-morpholinosulfonyl-2-n-propoxyphenyl)-1-n-prop yl-1,5-dihydro- 4H-pyrazolo[3,4-d]pyrimidin-4-one;

6-[5-(2-carboxyvinyl)-2-n-propoxyphenyl)-3-methyl-1-n-propyl -1,5-dihydro-4H -pyrazolo[3,4-d]pyrimidin-4-one;

6-[5-(2-t-butoxycarbonylvinyl)-2-n-propoxyphenyl]-3-methyl-1 -n-propyl-1,5-d ihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one;

3-methyl-6-[5-(2-morpholinocarbonylvinyl)-2-n-propoxyphenyl] -1-n-propyl-1,5 -dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one; and

3-methyl-6-[5-(2-morpholinocarbonylethyl)-2-n-propoxyphenyl] -1-n-propyl-1,5 -dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one.

Preferred compounds of formula (VIII) include those wherein R 65 is H, methyl or ethyl; and R 56 is C 1 -C 6 alkyl optionally substituted with cyclohexyl or with morpholino.

Preferred individual compounds of formula (VIII) include:

5-[2-ethoxy-5-(3-morpholinopropylsulfamoyl)-phenyl]-1,3-dime thyl-1,6-dihydr o-7H-pyrazolo[4,3-d]pyrimidin-7-one;

1-ethyl-5-[5-(n-hexylsulfamoyl)-2-n-propoxyphenyl]-3-methyl- 1,6-dihydro-7H- pyrazolo[4,3-d]pyrimidin-7-one;

1-ethyl-5-(5-diethylsulfamoyl-2-n-propoxyphenyl)-3-methyl-1, 6-dihydro-7H-py razolo[4,3-d]pyrimidin-7-one; and

5-[5-(N-cyclohexylmethyl-N-methylsulfamoyl)-2-n-propoxypheny l]1-ethyl-3-met hyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one.

Preferred compounds of formula (IX) include those wherein: R 57 is (a) hydrogen or halogen, e.g., fluorine; or (b) hydrogen.

Preferred compounds of formula (IX) also include those wherein: R 58 is (a) hydrogen, C 1 -6 alkyl, halo C 1 -6 alkyl, C 3 -8 cycloalkyl, C 3 -8 cycloalkyl C 1 -3 alkyl, aryl C 1 -3 alkyl or heteroaryl C 1 -3 alkyl; (b) hydrogen, C 1 -4 alkyl, halo C 1 -4 alkyl, C 3 -6 cycloalkyl, C 3 -6 cycloalkylmethyl, pyridyl C 1 -3 alkyl, furyl C 1 -3 alkyl or optionally substituted benzyl, such as benzyl or halobenzyl, e.g., fluorobenzyl; or (c) C 1 -4 alkyl, e.g., methyl, ethyl, isopropyl and n-butyl, C 3 -6 cycloalkyl, e.g., cyclopentyl, or C 3 -6 cycloalkylmethyl, e.g., cyclopropylmethyl.

Preferred compounds of formula (IX) further include those wherein: R 59 is (a) an optionally substituted benzene, thiophene, furan, pyridine or naphthalene ring or an optionally substituted bicyclic ring ##STR12##

where m is 1 or 2 and X and Y are each CH 2 or O; (b) a substituted benzene ring such as benzene substituted by C 1 -3 alkoxy, e.g., methoxy, or by C 1 -3 alkoxy and by halogen, e.g., chlorine, or preferably, 4-methoxyphenyl or 3-chloro-4-methoxyphenyl; or (c) 3,4-methylenedioxyphenyl.

Preferred compounds of formula (IX) further yet indude those wherein: R 60 is hydrogen, or R 58 and R 60 together are a 3-membered alkyl chain.

Preferred individual compounds of formula (IX) include:

cis-2,3,6,7,12,12a-hexahydro-2-(4-pyridylmethyl)-6-(3,4-meth ylenedioxypheny l)-pyrazino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione;

cis-2,3,6,7,12,12a-hexahydro-6-(2,3-dihydrobenzo[b]furan-5-y l)-2-methyl-pyr azino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione;

cis-2,3,6,7,12,12a-hexahydro-6-(5-bromo-2-thienyl)-2-methyl- pyrazino[2',1': 6,1]pyrido[3,4-b]indole-1,4-dione;

cis-2,3,6,7,12,12a-hexahydro-2-butyl-6-(4-methylphenyl)pyraz ino[2',1': 6,1]pyrido[3,4-b]indole-1,4-dione;

cis-2,3,6,7,12,12a-hexahydro-2-cyclopropyl-6-(3,4-methylened ioxy-phenyl)-py razino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione;

(3S,6R,12aR)-2,3,6,7,12,12a-hexahydro-3-methyl-6-(3,4-methyl enedioxyphenyl) -pyrazino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione;

(3S ,6R,12aR)-2,3,6,7,12,12a-hexahydro-2,3-dimethyl-6-(3,4-methy lenedioxypheny l)-pyrazino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione;

(6R,12aR)-2,3,6,7,12,12a-hexahydro-2-isopropyl-6-(3,4-methyl enedioxyphenyl) -pyrazino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione;

(6R,12aR)-2,3,6,7,12,12a-hexahydro-2-cyclopentyl-6-(3,4-meth ylenedioxypheny l)-pyrazino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione;

(6R,12aR)-2,3,6,7,12,12a-hexahydro-2-cyclopropylmethyl-6-(4- methoxyphenyl)- pyrazino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione;

(6R,12aR)-2,3,6,7,12,12a-hexahydro-6-(3-chloro-4-methoxyphen yl)-2-methyl-py razino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione;

(6R,12aR)-2,3,6,7,12,12a-hexahydro-2-methyl-6-(3,4-methylene dioxyphenyl)-py razino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione;

(6R,12aR)-2,3,6,7,12,12a-hexahydro-6-(3,4-methylenedioxyphen yl)-pyrazino[2' ,1':6,1]pyrido[3,4-b]indole-1,4-dione;

(5aR,12R,14aS)-1,2,3,5,6,11,12,14a-octahydro-12-(3,4-methyle nedioxyphenyl)- pyrrolo[1",2":4',5']pyrazino[2',1':6,1]pyrido[3,4-b]indole-5 -1,4-dione; and pharmaceutically acceptable salts thereof.

Particularly preferred individual compounds of formula (IX) are (6R,12aR)-2,3,6,7,12,12a-hexahydro-2-methyl-6-(3,4-methylene dioxyphenyl)-p yrazino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione and (3S,6R,12aR)-2,3,6,7,12,12a-hexahydro-2,3-dimethyl-6-(3,4-me thylenedioxyph enyl)-pyrazino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione, and the pharmaceutically acceptable salts thereof.

Preferred compounds of formulae (XA) and (XB) include those wherein: R 61 is C 1 -C 2 alkyl substituted with C 3 -C 5 cycloalkyl, CONR 65 R 66 or a N-linked heterocyclic group selected from pyrazolyl, triazolyl, morpholinyl and 4-R 67 -piperazinyl; (CH 2 ) p Het or (CH 2 ) q Ar; R 65 is H; R 66 is C 1 -C 4 alkyl optionally substituted with C 1 -C 4 alkoxy, or, R 65 and R 66 together with the nitrogen atom to which they are attached, form a morpholinyl group; Het is selected from pyridinyl, 1-oxidopyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, imidazolyl, isoxazolyl, thiazolyl, triazolyl and oxadiazolyl, any of which is optionally substituted with one or two substituents selected from C 3 , CH 2 CH 2 OCH 3 , OCH 3 and NH 2 .

Other preferred compounds of formulae (XA) and (XB) include those wherein: R 61 is C 1 -C 2 alkyl substituted with cyclobutyl, CONR 65 R 66 , pyrazol-1-yl, 1,2,3-triazol-1-yl, 1,2,4-triazol-1-yl, morpholin-4-yl or 4-methylpiperazin-1-yl; pyrimidin-2-yl; CH 2 Het or (CH 2 ) q Ar; R 62 is C 1 -C 3 alkyl; R 63 is C 1 -C 3 alkyl optionally substituted with C 1 -C 2 alkoxy; R 65 is H; R 66 is C 1 -C 2 alkyl optionally substituted with C 1 -C 2 alkoxy, or, R 65 and R 66 together with the nitrogen atom to which they are attached, form a morpholin-4-yl group; R 70 is C 1 -C 2 alkyl optionally monosubstituted with OH, OCH 3 or CONH 2 ; Het is selected from pyridin-2-yl, 1-oxidopyridin-2-yl, pyridin-3-yl, pyridazin-3-yl, pyridazin-4-yl, pyrimidin-4-yl, pyrimidin-5-yl, pyrazin-2-yl, 3-methoxypyridin-2-yl, 6-aminopyridin-2-yl, 1-methylimidazol-2-yl, 3,5-dimethylisoxazol-4-yl, 2-methylthiazol-4-yl, 1-methyl-1,2,4-triazol-5-yl, 1-(2-methoxyethyl)-1,2,4-triazol-5-yl, 4-methyl-1,2,4-triazol-3-yl, 3-methyl-1,2,4-triazol-5-yl, 1,2,4-oxadiazol-3-yl and 5-methyl-1,2,4-oxadiazol-3-yl; Ar is selected from phenyl, 4-chlorophenyl, 4-bromophenyl, 2-cyanophenyl, 2-carbamoylphenyl, 4-carbamoylphenyl, 2-nitrophenyl, 4-nitrophenyl, 2-aminophenyl, 4-aminophenyl, 2-methanesulfonamidophenyl, 4-methanesulfonamidophenyl, 4-ethanesulfonamidophenyl, 4-(prop-2-ylsulfonamido)phenyl and 4-sulfamoylphenyl.

Further preferred compounds of formulae (XA) and (XB) include those wherein: R 61 is cyclobutylmethyl, morpholin-4-ylcarbonylmethyl, 2-(morpholin-4-yl)ethyl, pyrimidin-2-yl, CH 2 Het or (CH 2 ) q Ar; R 62 is CH 2 CH 3 or CH 2 CH 2 CH 3 ; R 63 is CH 2 CH 3 , CH 2 CH 2 CH 3 or CH 2 CH 2 OCH 3 ; R 70 is CH 3 , CH 2 CH 3 or CH 2 CH 2 OH; Het is selected from pyridin-2-yl, pyridazin-3-yl, pyrazin-2-yl, 3-methoxypyridin-2-yl, 6-aminopyridin-2-yl, 1-methylimidazol-2-yl, 3,5-dimethylisoxazol-4-yl, 1-methyl-1,2,4-triazol-5-yl, 1-(2-methoxyethyl)-1,2,4-triazol-5-yl and 5-methyl-1,2,4-oxadiazol-3-yl; Ar is selected from phenyl, 2-aminophenyl, 2-methanesulfonamidophenyl, 4-methanesulfonamidophenyl, 4-ethanesulfonamidophenyl and 4-(prop-2-ylsulfonamido)phenyl.

Preferred individual compounds of formulae (XA) and (XB) include:

5-{5-[4-(2-hydroxyethyl)piperazin-1-ylsulfonyl]-2-n-propoxyp henyl}-3-n-prop yl-1-(pyridin-2-yl)methyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyri midin-7-one;

1-(1-methylimidazol-2-yl)methyl-5-[5-(4-methylpiperazin-1-yl sulfonyl)-2-n-p ropoxyphenyl]-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrim idin-7-one;

5-{5-[4-(2-hydroxyethyl)piperazin-1-ylsulfonyl]-2-n-propoxyp henyl}-3-n-prop yl-2-(pyridin-2-yl)methyl-2,6-dihydro-7H-pyrazolo[4,3-d]pyri midin-7-one;

5-[5-(4-ethylpiperazin-1-ylsulfonyl)-2-n-propoxyphenyl]-3-n- propyl-2-(pyrid in-2-yl)methyl-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one ;

3-ethyl-5-[5-(4-ethylpiperazin-1-ylsulfonyl)-2-n-propoxyphen yl]-2-(pyridin- 2-yl)methyl-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one;

5-[5-(4-ethylpiperazin-1-ylsulfonyl)-2-n-propoxyphenyl]-3-n- propyl-2-(pyrid azin-3-yl)methyl-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-o ne;

5-[5-(4-ethylpiperazin-1-ylsulfonyl)-2-n-propoxyphenyl]-3-n- propyl-2-(pyrid azin-2-yl)methyl-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-o ne; and

5-[2-ethoxy-5-(4-ethylpiperazin-1-ylsulfonyl)phenyl]-3-n-pro pyl-2-(pyridin- 2-yl)methyl-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one.

As discussed above, the compounds of the present invention possess cGMP PDE inhibitory activity and are described herein as useful in treating, e.g., preventing, reducing and/or reversing, nitrate-induced tolerance. Test methods for determining the cGMP PDE inhibitory activities of the compounds, or the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites or stereoisomers thereof, of the present invention can be understood and carried out by one skilled in the art in any suitable manner, e.g., according to one or more of the assays described in the aforementioned U.S. Pat. Nos. 5,250,534; 5,272,147; 5,294,612; 5,346,901; 5,488,055; 5,541,187; 5,614,530; 5,656,629; 5,482,941; 5,734,053; 5,736,548 and 5,591,742, and the International PCT Applications published as WO 93/06104; WO 93/07149; WO 93/12095; WO 94/00453; WO 94/05661; WO 94/28902; WO 95/19978; WO 96/16657; WO 96/28446; WO 96/28159; WO 96/28429; WO 96/28448; WO 97/03675 and WO 98/49166.

Test methods for determining the reduction and/or reversal of nitrate-induced tolerance of the compounds of formulae (I)-(XB) herein, or the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites or stereoisomers thereof, can be understood and carried out by one skilled in the art in any suitable manner, e.g., according to one or more of the assays described in the aforementioned U.S. Pat. Nos. 5,294,612; 5,488,055; 5,541,187; 5,614,530; 5,656,629 and 5,736,548, and International PCT Applications published as WO 96/28446; WO 96/28159; WO 96/28429; and WO 96/28448.

For administration to humans in the treatment, e.g., prophylactic, palliative, curative, prevention, reduction and/or reversal, of nitrate-induced tolerance, oral dosages of, e.g., a compound of formulae (I)-(XB), or any combination of the compounds of formulae (I)-(XB), or the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites or stereoisomers thereof (the active compounds), are generally in the range of from about 0.1 mg to about 1000 mg per day for an average adult patient (about 70 kg). Individual tablets or capsules should generally contain from about 0.1 mg to about 1000 mg of active compound, in a suitable pharmaceutically acceptable vehicle, diluent or carrier. Dosages for intravenous administration are typically within the range of from about 0.1 mg to about 500 mg per single dose as required. For intranasal or inhaler administration, the dosage is generally formulated as from about a 0.1% to about a 1% (w/v) solution. In practice, the physician will determine the actual dosage which will be most suitable for an individual patient and it will vary with age, weight and response of the particular patient. The above dosages are exemplary of the average case but there can, of course, be individual instances where higher or lower dosage ranges are merited, and all such dosages are within the scope of the present invention.

In addition, the treating physician will understand from the present disclosure how to select any suitable dosage of any suitable organic nitrate ester. For example, the treating physician will understand for any individual instance whether to lower the dosage of organic nitrate ester exemplary of the average case depending upon any suitable factors, e.g., when administering a particularly efficacious compound of the present invention where efficacious means the ability of the compound of the present invention to treat nitrate-induced tolerance.

For human use, the active compounds of the present invention can be administered alone, but will generally be administered in an admixture with a pharmaceutically acceptable vehicle, diluent or carrier selected with regard to the intended route of administration and standard pharmaceutical practice. For example, they may be administered orally in the form of tablets comprising such excipients as starch or lactose, or in capsules either alone or in admixture with excipients, or in the form of elixirs or suspensions comprising flavoring or coloring agents. They may be injected parenterally; for example, intravenously, intramuscularly or subcutaneously. For parenteral administration, they are best used in the form of a sterile aqueous solution which may contain other substances; for example, enough salts or glucose to make the solution isotonic.

Additionally, the active compounds may be administered topically and this may be done by way of creams, jellies, gels, pastes, and ointments, in accordance with standard pharmaceutical practice.

The active compounds may also be administered to a mammal other than a human such as, for example, a companion animal. The dosage to be administered will depend, for example, on the species and the disease or disorder being treated. The active compounds may be administered in the form of a capsule, bolus, tablet or liquid drench. The active compounds may also be administered by injection or as an implant. Such formulations are prepared in a conventional manner in accordance with standard veterinary practice. As an alternative, the compounds of the present invention may be administered with the feedstuff and for this purpose a concentrated feed additive or premix may be prepared for mixing with the normal feed.

The ability of the compounds, or the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites or stereoisomers thereof, of the novel methods and pharmaceutical compositions of the present invention, to inhibit cGMP PDE may be determined using a suitable method such as, for example, the assay described immediately below.

Compound affinities for cGMP and cAMP PDEs are assessed by determination of their IC 50 values (the concentration of inhibitor required for 50% inhibition of enzyme activity). The PDE enzymes are isolated from rabbit platelets and rat kidney, essentially by the method of W. J. Thompson and M. M. Appleman, Biochem. 10: 311 (1971). The calcium/calmodulin (Ca/CAM)-independent cGMP PDE and the cGMP-inhibited cAMP PDE enzymes are obtained from rabbit platelets while, of the four major PDE enzymes of the rat kidney, the Ca/CAM-dependent cGMP PDE (fraction I) is isolated. Assays are performed using a modification of the "batch" method of W. J. Thompson et al., Biochem. 18:5228 (1979).

The ability of the compounds, or the pharmaceutically acceptable salts, prodrugs, polymorphs, hydrates, solvates, active metabolites or stereoisomers thereof, of the novel methods and pharmaceutical compositions of the present invention, to reduce and/or reverse nitrate-induced tolerance may be determined using a suitable method such as, for example, the assay described immediately below.

Spontaneously hypertensive rats (from about 17 to about 25 weeks of age) are made nitroglycerin tolerant by repeated (three times per day for three consecutive days) administration (subcutaneously) of high doses of nitroglycerin (about 100 mg/kg). To confirm tolerance, challenge doses of nitroglycerin are administered (intravenously) at doses ranging from about 1 μg/kg to about 300 μg/kg and the maximum change in mean arterial pressure (MAP) for each dose is recorded.

Groups of tolerant rats are pretreated (intravenously) with representative compounds of the invention (tolerant pretreated group) or with vehicle (0.05N NaOH) (tolerant vehicle pretreated group) 5-10 minutes prior to the administration of challenge doses of nitroglycerin. A dose-MAP curve is generated, and the area under the dose-MAP curve is calculated for the non-tolerant group and for the tolerant vehicle pretreated group and the tolerant pretreated group. The percent reversal of nitrate-induced tolerance is calculated as follows: ##EQU1##

wherein: AUC tol -pretreated is the area under the dose-MAP curve for the tolerant pretreated group; AUC tol -veh is the area under the dose-MAP curve for the tolerant vehicle pretreated group; and AUC nontol is the area under the dose-MAP curve for the non-tolerant group. A percent reversal of 100% or greater indicates that a complete reversal of nitrate-induced tolerance has occurred, while a percent reversal of 0% indicates that no reversal of nitrate-induced tolerance has occurred.





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